SNP - dbSNP |
dbSNP | Type | Alleles | Het | Se(het) | Fxn-class | Gene Name | Assembly | Chr-pos | Sequence | Entrez Gene |
rs731237 | snp | C/G | 0 | 0 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852635 | GGCAGTCGGCCTTGT[C/G]TGCCGCGCACGGCTC | 8078 |
rs743599 | snp | C/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853136 | ATGTCACCCTCAAGC[C/G]GAGGCCCTTTGGGGC | 8078 |
rs1076865 | snp | C/T | 0.263181 | 0.249652 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853814 | TAGAGCATTTCTCAC[C/T]GGGGAGGTCAACTAA | 8078 |
rs1076866 | snp | C/T | 0.00943375 | 0.0680285 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853980 | TTGAGCAACAACAGA[C/T]ATCCTCTTCCAGGAA | 8078 |
rs1126996 | snp | A/G | 6.58924e-05 | 0.0057395 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6859512 | CCAGAATGCCCCGAC[A/G]GACCCTACCCAGGAT | 8078 |
rs1802898 | snp | C/T | | | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861076 | TACATCATGCAGCTG[C/T]CTGTGCCCATGGATG | 8078 |
rs2071058 | snp | A/T | 0.497566 | 0.0347987 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851729 | CTGGATACCCCCTTT[A/T]CAAATACCAAGACAA | 8078 |
rs2071059 | snp | A/G | 0.442197 | 0.159876 | intron-variant | USP5 | GRCh38.p7 | 12:6860567 | CCCATTTCTCCCTCT[A/G]TCAGCCCCAACCCAG | 8078 |
rs2071060 | snp | A/C | 0.0239773 | 0.106835 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864473 | GGTGGGCGGATCACG[A/C]GGTCAGCAGATCAAG | 8078 |
rs2071061 | snp | A/G | 0.277778 | 0.248452 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864487 | GCGGTCAGCAGATCA[A/G]GACCATCCTGGCTAA | 8078 |
rs2071062 | snp | C/T | 0.5 | 0 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864557 | AACCAAGCGTGGTGG[C/T]GGGCGTCTGTAGTCC | 8078 |
rs2071063 | snp | A/T | 0.0232526 | 0.105288 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864602 | GCTGAGGCAGGAGAA[A/T]GGCGTGAACCCGGGA | 8078 |
rs2071064 | snp | C/T | 0.230067 | 0.249204 | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866342 | CCCTGCCCCCGGAAT[C/T]CACAGTGCTCTGCTT | 8078 |
rs2226955 | snp | A/G | 0.463417 | 0.130205 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6856030 | AGGTGTTGAAGGCGG[A/G]TTTGACCTTAGCGAG | 8078 |
rs2238114 | snp | A/C | 0.491493 | 0.0646602 | intron-variant | USP5 | GRCh38.p7 | 12:6856576 | GCTTGGAAATGAACA[A/C]GACATGGGGATGGCC | 8078 |
rs2269356 | snp | A/G | 0.18176 | 0.243942 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6852447 | TGCCTTTCATTAACT[A/G]CGGCTGTCGTGTGAC | 8078 |
rs3182461 | snp | A/C | 0 | 0 | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866604 | AAAATGCCAAAATAC[A/C]CGATGTGAATAAAAG | 8078 |
rs4334119 | snp | A/C | 0.203509 | 0.245639 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6866863 | TCCACTCCTGTGTGA[A/C]TAAAGAGAGGGAAGG | 8078 |
rs5796253 | in-del | -/CA/TG | | | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850161 | CACACACACACACAA[-/CA/TG]AAAGCACGGTGGCAT | 8078 |
rs7976501 | snp | A/G | 0.0413113 | 0.137656 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851860 | GAATGGACTCTAAGG[A/G]TCCCGGAGCCGGAGC | 8078 |
rs10744719 | snp | C/T | 0 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6854954 | GTCTTTCCTCTCCCA[C/T]GAAGGGACCCTTTTT | 8078 |
rs10744720 | snp | C/T | 0.131423 | 0.22009 | intron-variant | USP5 | GRCh38.p7 | 12:6855049 | CTGTTAGCCCCAGGA[C/T]AGAGGTGAAGGAAGT | 8078 |
rs11064431 | snp | C/G | 0.236032 | 0.24961 | intron-variant | USP5 | GRCh38.p7 | 12:6854375 | ACAAGTCATTGTTCC[C/G]CTGGAAGCCACACTT | 8078 |
rs11064432 | snp | C/G | 0.261687 | 0.249733 | intron-variant | USP5 | GRCh38.p7 | 12:6859577 | TAGGAAAGCTGTTGA[C/G]AGTCATGGCCGTATA | 8078 |
rs11064433 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864353 | GGAGCTGAAGCCTGC[A/G]TTCACTGCTGGGTTT | 8078 |
rs11551593 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851865 | CAGCTGCTCCGGCTC[A/C]GGGACCCTTAGAGTC | 8078 |
rs11609766 | snp | A/C | | | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851912 | GCAACCCCGAAGCCC[A/C]CCTAGCTGCTCTACG | 8078 |
rs11612543 | snp | A/G | 0.110497 | 0.207458 | intron-variant | USP5 | GRCh38.p7 | 12:6858737 | AGAGTAGTTCCTATC[A/G]GCTGGGTGTGTTGGC | 8078 |
rs11830318 | snp | A/C | 0.0434404 | 0.14083 | intron-variant | USP5 | GRCh38.p7 | 12:6860538 | TTCCTGCAATTTACT[A/C]GCTCTCCTTCCTGCC | 8078 |
rs11832410 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858836 | ccagcctgggcaaca[C/T]agcgagaccctgtct | 8078 |
rs11832671 | snp | A/G | 0.0917839 | 0.193566 | intron-variant | USP5 | GRCh38.p7 | 12:6860308 | CTGGGAGATGTCTAA[A/G]GAAGGCCCCTGGATG | 8078 |
rs12302749 | snp | C/T | 0.43634 | 0.166666 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6867132 | AAGGAGGTTGTCTAT[C/T]CCACAGTTGGAGAGG | 8078 |
rs12824102 | snp | C/T | 0.0465639 | 0.145306 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863924 | CTACACGGGCAACAG[C/T]GGGGCTGAGGCCGCC | 8078 |
rs16932955 | snp | A/G | 0.022469 | 0.103584 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851508 | GCCTGCGAGCCGTCC[A/G]TGGCAGGCTGAGGAG | 8078 |
rs17788417 | snp | C/T | 0.00986232 | 0.0695262 | intron-variant | USP5 | GRCh38.p7 | 12:6860315 | ATGTCTAAAGAAGGC[C/T]CCTGGATGGCCACTG | 8078 |
rs17790720 | snp | C/T | 0.0546152 | 0.155964 | intron-variant | USP5 | GRCh38.p7 | 12:6860824 | ATTAGGGAAGGTTTC[C/T]GCTCTGCTCTTGTGT | 8078 |
rs35165406 | snp | A/G | 0.0138207 | 0.0819715 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863250 | CAGCTCCTCCTCTCC[A/G]GGCTGCAGCCCTGTG | 8078 |
rs56405548 | snp | A/C | | | intron-variant | USP5 | GRCh38.p7 | 12:6858323 | GTAATTCCACAAATT[A/C]TAGGCCACAGTTGAG | 8078 |
rs58321642 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859101 | AGGAGGGGGGCTTGG[C/T]ACACTAAGAATAAAG | 8078 |
rs60219247 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6866740 | TGCCAAAGTCAAGTC[C/T]CCACTTTTCACTGGT | 8078 |
rs60975689 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859221 | TAGAACGTGAACTGC[A/G]CTTATCCTAATCCCA | 8078 |
rs61607719 | snp | C/G | | | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864612 | GAGAAAGGCGTGAAC[C/G]CGGGAGGCGGAGCTT | 8078 |
rs61761597 | snp | C/T | 0.000131917 | 0.00812043 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6863248 | GGCACAGGGCTGCAG[C/T]CCGGAGAGGAGGAGC | 8078 |
rs61916318 | snp | A/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6859818 | CCACCACGCCCAGCT[A/T]AATTTTTTTTGTATT | 8078 |
rs66621175 | snp | C/T | 0.444444 | 0.157135 | intron-variant | USP5 | GRCh38.p7 | 12:6856641 | GGGCCTGCAGAGCCC[C/T]CTCTCTCTGCCACTC | 8078 |
rs72653460 | snp | C/T | 0.299444 | 0.245062 | intron-variant | USP5 | GRCh38.p7 | 12:6858681 | CTGGGCATACTCCTC[C/T]TTCAGCTTCCCTCAG | 8078 |
rs73260817 | snp | A/C | 0.5 | 0 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851694 | AGTCACTCGACACAA[A/C]CCCCTCAAGCTCCGC | 8078 |
rs73260823 | snp | A/G | 0.0333766 | 0.124797 | intron-variant | USP5 | GRCh38.p7 | 12:6855371 | CTTCATAACATCCTC[A/G]TGTTTTCACCCTTAC | 8078 |
rs73260825 | snp | C/T | 0.444444 | 0.157135 | intron-variant | USP5 | GRCh38.p7 | 12:6857393 | CTTATCCTATACAGG[C/T]AGAATCAGAATCACA | 8078 |
rs73260833 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6860079 | GGGAGAGCCACGAGC[A/G]GGGGGTTGAGCTGGG | 8078 |
rs73260840 | snp | C/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6865809 | AGACATAATAGGGTC[C/T]GTGACCCTTGTGAGG | 8078 |
rs74505435 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859610 | TTCCTCCTCCCTGAC[C/T]GCCTGGGGGGCACAG | 8078 |
rs76061250 | snp | A/T | 0.5 | 0 | upstream-variant-2KB, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6850193 | TGTTATGTGTGTGTA[A/T]TTTTTCTAGAGATGG | 8078 |
rs76083908 | snp | C/T | 0.0133132 | 0.0804944 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860158 | TAATGCAGGGCCAAG[C/T]TGGGCCATGGCCTTC | 8078 |
rs77625565 | snp | C/G | | | intron-variant, upstream-variant-2KB | USP5, TPI1 | GRCh38.p7 | 12:6865473 | TCACTATGTTGCCCA[C/G]GCTGGTCTTGAACTC | 8078 |
rs78059433 | snp | A/G | 0.04875 | 0.148319 | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866606 | AATGCCAAAATACAC[A/G]ATGTGAATAAAAGTA | 8078 |
rs78835987 | snp | C/G | 0.0350586 | 0.127672 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864241 | CCAGTGGGGAAGAAG[C/G]GGGTGGGAATGAGGG | 8078 |
rs79239224 | snp | A/T | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP5, TPI1 | GRCh38.p7 | 12:6865444 | CAGCTTTTTTTTTAA[A/T]TAGAGATGGGATCTC | 8078 |
rs79430235 | snp | A/C | 0.000191543 | 0.0097844 | missense, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861475 | GAGGAGAAGAAGCGG[A/C]AAGCCGAAGAGGAGA | 8078 |
rs79451772 | snp | A/G | 0.000414212 | 0.0143852 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860461 | GCAGGATGCCCAGGA[A/G]TTCTTCCTTCACCTT | 8078 |
rs111457078 | snp | A/G | 0.48 | 0.0979796 | intron-variant | USP5 | GRCh38.p7 | 12:6859789 | TCCTGAGTAGCTAGG[A/G]CTACAGGCACATGCC | 8078 |
rs111560611 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6854195 | TCTCAGCAAGTGTTG[C/T]GAGATTGTTGTCAGA | 8078 |
rs111601142 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6863439 | GCCTCTCTGCCTTGC[A/G]TCCCCTGCCCCTGTC | 8078 |
rs112029690 | snp | A/G | 0.000577997 | 0.0169901 | intron-variant | USP5 | GRCh38.p7 | 12:6861642 | CTGGTCGGGGCCTGA[A/G]GCTGTGGGTCTATGG | 8078 |
rs112218165 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859906 | GTGGTCTGCCCACCT[C/T]GGCCTCCCAAAGTGC | 8078 |
rs112300530 | snp | C/G/T | 0.00668249 | 0.0574159 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864217 | GCTGCCCCAGCTAAG[C/G/T]ACATGGGGCCAGTGG | 8078 |
rs112306827 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6858858 | ACCCTGTCTTCTCTT[A/G]AAAAAAAAAAAGAAT | 8078 |
rs112511011 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6854474 | AGAAAGGTCTTTTTC[A/G]CTGGATGTTTAGTCT | 8078 |
rs112562622 | snp | A/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6861259 | AGGTAGATTAACCTC[A/G]TCCAGTGGACACTCA | 8078 |
rs112657515 | snp | A/C/G | 0 | 0 | splice-acceptor-variant | USP5 | GRCh38.p7 | 12:6859469 | TTCCCTTGACTTTTA[A/C/G]GTATGTGGATAAGCT | 8078 |
rs112930588 | snp | C/T | 0.00229659 | 0.0338086 | intron-variant | USP5 | GRCh38.p7 | 12:6860511 | GGGCTGGCAAGATGG[C/T]ACACCCCCATCTTCC | 8078 |
rs113032589 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6854681 | AAGGATCACTTGAGC[C/T]GGGGAGGTTGAGGCT | 8078 |
rs113045682 | snp | C/T | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6855151 | GCTGTTGAATGGCGA[C/T]GATGAGCTGGTGTTC | 8078 |
rs113090296 | snp | A/T | 0.5 | 0 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864581 | GTAGTCCCAGCTACT[A/T]GGGAGGCTGAGGCAG | 8078 |
rs113159521 | snp | A/G | 0 | 0 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864422 | TGGCCGGGCGCGGTG[A/G]CTCACGCCTGTAATC | 8078 |
rs113206881 | snp | C/T | 0 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6861304 | CTGCATGGAAACAGG[C/T]GAGATATATTGGACA | 8078 |
rs113208756 | in-del | -/A | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6858858 | ACCCTGTCTTCTCTT[-/A]AAAAAAAAAAAGAAT | 8078 |
rs113356469 | snp | A/C | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859203 | TCAACAGGTTCTGTC[A/C]AATAGAACGTGAACT | 8078 |
rs113502733 | snp | C/G | 0.5 | 0 | upstream-variant-2KB, intron-variant | TPI1, USP5 | GRCh38.p7 | 12:6866919 | CTAGCTGGCTTCAGG[C/G]TGGGACTCAGTCCCT | 8078 |
rs113542671 | snp | A/G/T | 0 | 0 | upstream-variant-2KB, splice-acceptor-variant, intron-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851011 | CGAGGAGGGAATGCC[A/G/T]GTGAGAAGTGACTCA | 8078 |
rs113561440 | snp | A/G | 0.5 | 0 | intron-variant, downstream-variant-500B | USP5 | GRCh38.p7 | 12:6864465 | GAGGGTGAGGTGGGC[A/G]GATCACGCGGTCAGC | 8078 |
rs113655717 | snp | C/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6859743 | CTACAACCTCTGCCT[C/G]CTGGGTTCAAGTGAT | 8078 |
rs113823591 | snp | C/G | 0.5 | 0 | intron-variant | USP5 | GRCh38.p7 | 12:6862766 | GATTTACAACCAAAA[C/G]TGATTTTTGTAGTTT | 8078 |
rs113894137 | snp | A/G | 0.5 | 0 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853455 | AAAAGAGCACTGCGC[A/G]GAGCAGAGCTCCGGG | 8078 |
rs114210148 | snp | C/T | | | intron-variant | USP5 | GRCh38.p7 | 12:6858346 | CAGTTGAGTATCATC[C/T]TAGACTCAGTGAGAG | 8078 |
rs114350224 | snp | A/G | 0.000313255 | 0.0125112 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6857681 | CCCCAGCCTGGCTGA[A/G]CACCTGTCCCACTTC | 8078 |
rs114768694 | snp | C/T | 0.0654984 | 0.168698 | intron-variant | USP5 | GRCh38.p7 | 12:6862254 | CCTGGGCTTTTTTCT[C/T]TTTCTTTTTTTTGTT | 8078 |
rs114840368 | snp | A/G | 0.096524 | 0.197345 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853756 | GCTAACCAACTTCCA[A/G]CATATTTGGTTACCT | 8078 |
rs114987450 | snp | A/C | 0.0333238 | 0.124705 | intron-variant, upstream-variant-2KB | USP5, CDCA3 | GRCh38.p7 | 12:6853933 | TTTTTCATATCACAG[A/C]AGAGAAATGTTCAAG | 8078 |
rs115270213 | snp | A/G | 0.0333238 | 0.124705 | intron-variant | USP5 | GRCh38.p7 | 12:6856244 | AAGCTGAAGGCCAAG[A/G]GGAAGAGGGGCATGT | 8078 |
rs115306507 | snp | A/C | 0.00398963 | 0.0444848 | intron-variant | USP5 | GRCh38.p7 | 12:6857601 | CCTGAGCCACTTCCC[A/C]TGATTCTCTTCCTGC | 8078 |
rs115578303 | snp | C/G | 0.0333238 | 0.124705 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6852036 | GGCGGAGCACCGGCA[C/G]GCAGGCTCCGTCCAA | 8078 |
rs115612078 | snp | C/T | 0.00214518 | 0.0326801 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6860410 | GTTCAAGGCCCTCAT[C/T]GGCAAGGGCCACCCT | 8078 |
rs115666159 | snp | G/T | 0.0038981 | 0.0439756 | intron-variant | USP5 | GRCh38.p7 | 12:6855562 | AGGCCTGGGTACATT[G/T]TCTGTTCCATTCTGA | 8078 |
rs115858711 | snp | A/G | 0.0495547 | 0.149404 | upstream-variant-2KB, utr-variant-5-prime, nc-transcript-variant | USP5, CDCA3 | GRCh38.p7 | 12:6851832 | AGTTCCTGCTCTTCA[A/G]TAGAAGGCACGCGAA | 8078 |
rs116196909 | snp | A/G | 0.0168055 | 0.0901129 | intron-variant | USP5 | GRCh38.p7 | 12:6860750 | AAGAAAAATACAAGC[A/G]TGTTCTAACACAGTC | 8078 |
rs116418094 | snp | A/G/T | 0.0134541 | 0.0809187 | intron-variant | USP5 | GRCh38.p7 | 12:6863801 | GTGGCCCAATCAGTC[A/G/T]GTCCGTGTACCCACA | 8078 |
rs117876102 | snp | A/G | 0.00456116 | 0.0475371 | synonymous-codon, nc-transcript-variant | USP5 | GRCh38.p7 | 12:6861471 | GTACGAGGAGAAGAA[A/G]CGGCAAGCCGAAGAG | 8078 |
rs137961270 | snp | C/T | 0.000165158 | 0.0090858 | synonymous-codon | USP5 | GRCh38.p7 | 12:6864820 | GGGCCGCTCAGCTGC[C/T]GACTCCATCTCTGAG | 8078 |
rs138130918 | snp | C/G | | | upstream-variant-2KB, utr-variant-3-prime | TPI1, USP5 | GRCh38.p7 | 12:6866420 | TTTGTGCGCGTGGGT[C/G]TAGCTTTGTGCATCC | 8078 |